Chott A, Vesely M, Simonitsch I, Mosberger I, Hanak H
Department of Clinical Pathology, University of Vienna, Austria.
Am J Clin Pathol. 1999 Jan;111(1 Suppl 1):S68-74.
We studied 42 intestinal T-cell lymphomas (ITLs) to establish a simple and reproducible classification. The ITLs were classified into pleomorphic small cell (n = 3), monomorphic medium-sized cell (n = 10), pleomorphic medium and large cell (n = 17), immunoblastic (n = 1), and anaplastic large cell (n = 9) lymphomas. Two cases were unclassifiable. Overlapping histologic features were noted between some cases and also within the same tumor and between multiple lesions of the same patient. Histologic evidence of enteropathy was present in most cases. The ITLs expressed cytoplasmic CD3 and antigens associated with cytolytic function (TIA-1, granzyme B), but not CD4 and CD5. Six of the 10 monomorphic medium-sized cell lymphomas were CD56+ T-cell lymphomas. Because of the histologic heterogeneity in some ITLs, we suggest a classification system with 2 main categories: (1) small to medium-sized cell, comprising pleomorphic small and monomorphic medium-sized cell lymphomas; and (2) large cell, comprising the remaining subtypes. The differential diagnosis includes B-cell lymphomas, tumors of histiocytic origin, anaplastic carcinoma, and malignant melanoma.
我们研究了42例肠道T细胞淋巴瘤(ITL),以建立一个简单且可重复的分类系统。这些ITL被分为多形性小细胞淋巴瘤(n = 3)、单形性中等大小细胞淋巴瘤(n = 10)、多形性中等和大细胞淋巴瘤(n = 17)、免疫母细胞淋巴瘤(n = 1)以及间变性大细胞淋巴瘤(n = 9)。有2例无法分类。在一些病例之间、同一肿瘤内部以及同一患者的多个病灶之间均发现了重叠的组织学特征。大多数病例存在肠病的组织学证据。ITL表达细胞质CD3以及与细胞溶解功能相关的抗原(TIA-1、颗粒酶B),但不表达CD4和CD5。10例单形性中等大小细胞淋巴瘤中有6例为CD56 + T细胞淋巴瘤。由于部分ITL存在组织学异质性,我们建议采用一个包含2个主要类别的分类系统:(1)小至中等大小细胞型,包括多形性小细胞和单形性中等大小细胞淋巴瘤;(2)大细胞型,包括其余亚型。鉴别诊断包括B细胞淋巴瘤、组织细胞起源的肿瘤、间变性癌和恶性黑色素瘤。